Interactions of Cationic Lipids with DNA: A Structural Approach

Langmuir. 2018 Dec 11;34(49):14858-14868. doi: 10.1021/acs.langmuir.8b01635. Epub 2018 Sep 13.

Abstract

Colloidal nucleic acid carrier systems based on cationic lipids are a promising pharmaceutical tool in the implementation of gene therapeutic strategies. This study demonstrates the complex behavior of DNA at the lipid-solvent interface facilitating structural changes of the lyotropic liquid-crystalline phases. For this study, the structural properties of six malonic acid based cationic lipids were determined using small- and wide-angle X-ray scattering (SAXS and WAXS) as well as differential scanning calorimetry (DSC). Selected lipids (lipid 3 and lipid 6) with high nucleic acid transfer activity have been investigated in detail because of the strong influence of the zwitterionic helper lipid 1,2-di(9 Z-octadecenoyl)- sn-glycero-3-phosphoethanolamine (DOPE) on the structural properties as well as of the complex formation of lipid-DNA complexes (lipoplexes). In the case of lipid 3, DNA stabilizes a metastable cubic mesophase with Im3 m symmetry and an Im3 m Qαc lipoplex is formed, which is rarely described for DNA lipoplexes in literature. In the case of lipid 6, a cubic mesophase with Im3 m symmetry turns into a fluid lamellar phase while mixing with DOPE and complexing DNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amides / chemistry*
  • DNA / chemistry*
  • Fatty Acids, Unsaturated / chemistry*
  • Malonates / chemistry*
  • Molecular Structure
  • Scattering, Small Angle
  • Thermodynamics
  • Transition Temperature
  • X-Ray Diffraction

Substances

  • Amides
  • Fatty Acids, Unsaturated
  • Malonates
  • DNA